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Enterobacteriaceae

 Enterobacteriaceae (9830-11) Reinforce your knowledge and skills as you use nomenclature, cultural characteristics, identification techniques and pathogenicity to differentiate Escherichia, Shigella, Salmonella, Enterobacter and other clinically significant isolates.

Code 9830-11
Level Basic

Member Price

$0

Non-Member Price

$135

 

Additional Details

PEP hours: 8
CPS/ART credits: 0
 
Learning Outcomes:
Enterobacteriaceae
·       List the common characteristics of the family Enterobacteriaceae.
·       List the three Enterobacteriaceae most commonly isolated from clinical specimens.
Escherichia
·       Describe typical colonies on blood and MacConkey agar.
·       State typical reactions for:
       Glucose
       Lactose
       TSI
       ONPG
       Indole
       Voges-Proskauer
       Citrate
       Motility
       Lysine
·       State how rapid identification of E. coli may be carried out.
·       List infections commonly caused by E. coli.
·       List the four types that cause enteric disease
·       Know the significance of an ESBL producer.
Shigella
·       Name the genus most closely related to Shigella.
·       Describe colonies on MacConkey agar.
·       State the suitability of SS, XLD, HE, tetrathionate, selenite and GN broth for isolation of Shigella.
·       State typical reactions for:
       Motility
       Lactose
       Phenylalanine deaminase
       Glucose
       Sucrose
       Urease
·       State how species identification is established.
·       Describe the procedure for serogrouping.
·       Explain why serotyping would be done.
·       Describe the pathogenicity.
Edwardsiella
·       State reactions that would distinguish Edwardsiella from E. coli and from Salmonella species.
·       State the clinical significance.
Salmonella
·       Describe typical colonies on Mac, SS, XLD, SS, HE and bismuth sulfide media.
·       State typical reactions for:
       Glucose
       TSI
       Motility
       Indole
       Citrate
       Phenylalanine deaminase
       Urease
       ONPG
       Lysine decarboxylase
·       State reactions that may differentiate S. typhi from other Salmonella species.
·       Outline the steps in serological identification.
·       Describe the infection caused by S. typhi and state what specimens are best for diagnosis at various stages of disease.
·       Describe the pathogenicity of the other Salmonella species and state the specimen required for diagnosis.
·       State the usual bacterial reservoir of Salmonella species.
Citrobacter
·       Compare reactions of Citrobacter freundii with those of Salmonella species in:
       TSI
       ONPG
       Lysine decarboxylase
·       Describe the pathogenicity of Citrobacter
Klebsiella
·       Name the two most commonly isolated species.
·       Describe typical colonies on MacConkey agar and state the incidence of capsules.
·       State typical reactions for K. pneumoniae and K. oxytoca for:
       Glucose
       Lactose
       TSI
       Motility
       Citrate
       Indole
       Ornithine decarboxylase
·       List common infections and describe the role of Klebsiella in nosocomial infections.
Enterobacter
·       Name the two species most commonly isolated from clinical material.
·       Describe typical colonies of Enterobacter aerogenes and E. cloacae on MacConkey agar.
·       State the colour of pigment produced by E. sakazakii and Pantoea (Enterobacter) agglomerans.
·       State typical reactions of Enterobacter aerogenes and E. cloacae for:
       Glucose
       Lactose
       TSI
       Motility
       Citrate
       Indole
       Ornithine decarboxylase
·       Describe the clinical significance of Enterobacter aerogenes, E. cloacae and E. sakazakii.
Hafnia
·       State the genus most similar to Hafnia in biochemical reactions.
·       Describe typical colonies on MacConkey agar. Compare Hafnia and Shigella in the following tests:
       TSI
       Motility
       Shigella Antisera
·       State the clinical significance
Serratia
·       Name the species most commonly isolated from clinical material.
·       Describe the pigment occasionally seen.
·       Describe colonies on MacConkey agar.
·       State reactions of Serratia marcescens for:
       DNase
       Glucose
       Lactose
       Sucrose
       TSI
       Phenylalanine deaminase
       Arabinose
·       Describe the pathogenicity of S.marcescens and its role in nosocomial infections
Proteus
·       Name the three species recognized as human pathogens
·       Describe typical colonies on blood, MacConkey and stool media
·       State typical reactions for:
       Glucose
       Lactose
       Sucrose
       H2S
       TSI
       Phenylalanine deaminase
       Urease
       Indole
·      State the significance in stool cultures
·      Describe pathogenicity
Morganella
·       Name the one species
·       Describe colonies on blood and MacConkey agar
·       State typical reactions for:
       Glucose
       Lactose
       Sucrose
       H2S
       TSI
       Phenylalanine deaminase
       Urease
·       Describe the clinical significance
Providencia
·       Name the two species most often isolated from clinical specimens
·       Describe colonies on blood and MacConkey agar
·       State typical reactions for:
       Glucose
       Lactose
       Sucrose
       H2S
       TSI
       Phenylalanine deaminase
       Urease
·       Describe the clinical significance
Yersinia
·       Name the three species that are well recognized as human pathogens.
·       State the optimum temperature range for growth.
·       Describe the suitability of the following media for isolation of Y. enterocolitica:
       Blood agar
       MacConkey agar
       SS agar
       Cold enrichment
       CIN agar
·       Describe typical colonies of Y. enterocolitica on blood and CIN agar.
·       List six characteristics that may indicate Y. enterocolitica.
·       Describe the pathogenicity of Y. pestis, Y. enterocolitica and Y. pseudotuberculosis.
 
Instructor: Helen Smith, MLT
Prerequisites: None
Textbook: N/A
Equipment: Computer with Internet is required
Start Date: Upon registration
Completion: Up to 52 weeks
Version Date: December 2011